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BioWorld - Thursday, May 7, 2026
Home » Topics » Cancer, BioWorld

Cancer, BioWorld
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ASCO20: Enhertu improves overall survival in metastatic gastric cancer

June 1, 2020
By Lee Landenberger
The juggernaut that is Daiichi Sankyo Co. Ltd.’s Enhertu continued to roll into this weekend’s American Society of Clinical Oncology virtual meeting, bringing momentum from its December FDA approval for HER2-positive breast cancer, along with fresh data from three new studies in other indications.
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Repare’s Bristol Myers Squibb deal worth up to $3B

May 30, 2020
By Lee Landenberger
In a deal potentially worth $3 billion, privately held Repare Therapeutics Inc., of Cambridge, Mass., and Montreal, entered a research collaboration with Bristol Myers Squibb Co. (BMS) to identify synthetic lethal precision oncology targets for drug candidates.
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Preclinical ASCO data lift RNAi firm Phio’s shares

May 29, 2020
By Lee Landenberger
Positive preclinical data from Phio Pharmaceuticals Inc., of Marlborough, Mass., propelled the company stock (NASDAQ:PHIO) dramatically upward, about 86%, at midday Friday only to see it finally settle at a more modest 36.16% increase to close May 29 at $3.05.
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Lung cancer illustration

Just Adaurable: Astrazeneca’s phase III Tagrisso data captivate at ASCO

May 29, 2020
By Randy Osborne
Astrazeneca plc’s Tagrisso (osimertinib) seems poised to become standard of care in the adjuvant setting for early stage (IB, II and IIIA) EGFR-mutated non-small-cell lung cancer (NSCLC), thanks to phase III data from the study called Adaura, made public at the American Society of Clinical Oncology (ASCO) meeting.
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Imminent Ebola vaccine approval in Europe a historic first for J&J’s Advac platform

May 29, 2020
By Cormac Sheridan
DUBLIN – Johnson & Johnson’s Janssen Biotech arm is on the brink of a historic first vaccine approval, having secured a positive vote May 29 from the EMA’s Committee for Medicinal Products for Human Use (CHMP) for its prime-boost Ebola virus vaccine combo, Zabdeno (Ad26.Zebov) plus MVABEA (MVA-BN-Filo).
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Qurient to start phase I trials for triple kinase inhibitor Q-702

May 29, 2020
By Gina Lee
HONG KONG – South Korea’s Qurient Co. Ltd., located in Gyeonggi-do, is preparing to send its novel drug, Q-702, into the clinic after receiving clearance from the U.S. FDA, roughly a month after submitting the application on April 24.
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ASCO analysis weighs cancer plus COVID-19 double whammy

May 28, 2020
By Randy Osborne
The impact of COVID-19 is being felt at the American Society of Clinical Oncology (ASCO) annual meeting as much as anywhere else, typically held at McCormick Place in Chicago but this year conducted virtually because of the pandemic.
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Wall Street sign

All eyes (virtually) focused on ASCO: Which companies will impress Wall Street?

May 28, 2020
By Peter Winter
The American Society of Clinical Oncology (ASCO) annual meeting will be closely watched by analysts and investors alike. There is no doubt that favorable data presented at the event will advance a company's stock valuation significantly. Equally, candidate cancer therapies that do not live up to expectations will see their developers face the ire of investors.
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CAR T cell attacking cancer cells

Edigene, Immunochina betting on allogeneic CAR T therapy in cancer collaboration

May 28, 2020
By Elise Mak
SUZHOU, China – Genome editing startup Edigene Inc. and CAR T developer Immunochina Pharmaceuticals Co. Ltd., both from Beijing, have unveiled joint efforts to develop an allogeneic CAR T therapy for cancer. Terms remain undisclosed.
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Hands holding gears

Gold, plated: Arcus covenant with Gilead commands potential $2B chestful

May 27, 2020
By Randy Osborne
Arcus Biosciences Inc. “brings the milk without [Gilead Sciences Inc.] having to buy the whole cow” is the way one analyst characterized the pair’s 10-year cancer immunotherapy deal, which could be worth as much as $2 billion, and some may have detected downside for Arcus, as shares (NYSE:RCUS) closed May 27 at $27.05, down $6.49, or 19%. Foster City, Calif.-based Gilead is paying Arcus, of Hayward, Calif., $175 million up front, shelling out a $200 million equity investment, and pledging potentially $1.6 billion or more in the form of R&D support, opt-in cash and milestone payments.
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